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HYPERGLYCAEMIA ( 26 FDA reports)
BLOOD GLUCOSE INCREASED ( 19 FDA reports)
HYPOGLYCAEMIA ( 14 FDA reports)
BLOOD GLUCOSE DECREASED ( 10 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
VISION BLURRED ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
MALAISE ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FALL ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
APHASIA ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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